Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report

por Cherkaoui Jaouad, Imane, Guaoua, Soukaina, Hajjioui, Aicha, Sefiani, Abdelaziz
Publicado 2014

Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report

por Sahli, Maryem, Zrhidri, Abdelali, Boualaoui, Imad, Cherkaoui Jaouad, Imane, El Kadiri, Youssef, Nouini, Yassine, Sefiani, Abdelaziz
Publicado 2023

Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report

por Cherkaoui Jaouad, Imane, El Alloussi, Mustapha, Chafai El alaoui, Siham, Laarabi, Fatima Zahra, Lyahyai, Jaber, Sefiani, Abdelaziz
Publicado 2015

A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report

por Cherkaoui Jaouad, Imane, Zrhidri, Abdelali, Jdioui, Wafaa, Lyahyai, Jaber, Raymond, Laure, Egéa, Grégory, Taoudi, Mohamed, El Mouatassim, Said, Sefiani, Abdelaziz
Publicado 2018

Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

por Benbouchta, Yahya, Cherkaoui Jaouad, Imane, Tazi, Habiba, Elorch, Hamza, Ouhenach, Mouna, Zrhidri, Abdelali, Sadki, Khalid, Sefiani, Abdelaziz, Lyahyai, Jaber, Berraho, Amina
Publicado 2021